NR4A1

Gene Information
 
Gene Symbol
NR4A1
 
Aliases
GFRP1, HMR, N10, NAK-1, NGFIB, NP10, NUR77, TR3
 
Entrez Gene ID
 
Gene Name
Nuclear receptor subfamily 4 group A member 1
 
Chromosomal Location
12q13.13
 
HGNC ID
 
Summary
This gene encodes a member of the steroid-thyroid hormone-retinoid receptor superfamily. Expression is induced by phytohemagglutinin in human lymphocytes and by serum stimulation of arrested fibroblasts. The encoded protein acts as a nuclear transcription factor. Translocation of the protein from the nucleus to mitochondria induces apoptosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
  e!Ensembl
Gene
Transcript  
Protein

Gene Ontology (GO)

GO ID Ontology Function Evidence Reference
GO:0001938 Biological process Positive regulation of endothelial cell proliferation IMP 18059339
GO:0002042 Biological process Cell migration involved in sprouting angiogenesis IDA 18059339
GO:0007165 Biological process Signal transduction TAS 2626032
GO:0035767 Biological process Endothelial cell chemotaxis IMP 18059339
GO:0035924 Biological process Cellular response to vascular endothelial growth factor stimulus IMP 18059339
Protein Information
 
Protein Name
Nuclear receptor subfamily 4 group A member 1, ST-59, TR3 orphan receptor, early response protein NAK1, growth factor-inducible nuclear protein N10, hormone receptor, nerve growth factor IB nuclear receptor variant 1, nuclear hormone receptor NUR/77, orphan nuclear receptor HMR, orphan nuclear receptor TR3, steroid receptor TR3, testicular receptor 3
 
Function
 
UniProt
 
PDB
 
Pfam
Pfam Accession Pfam ID
PF00104 Hormone_recep
PF00105 zf-C4
Pathways
 
KEGG
 
Reactome
 

MAPK signaling pathway
PI3K-Akt signaling pathway
Aldosterone synthesis and secretion
Cortisol synthesis and secretion
Cushing syndrome

 

AKT phosphorylates targets in the nucleus
Nuclear Receptor transcription pathway
Constitutive Signaling by AKT1 E17K in Cancer

Interactions
 
STRING MINT IntAct
ENSP00000440864 P22736 P22736
    View interactions
     

Associated Diseases

Disease groupDisease NameReferences
Blood Disorders
Myelodysplastic Syndrome
Cardiovascular Diseases
Ventricular Fibrillation
Atherosclerosis
Cardiomyopathy
Digestive System Diseases
Inflammatory Bowel Diseases
References
 
 
PubMed ID Associated gene/s Associated condition Genetic Mutation Diagnostic Criteria Association with PCOS Ethnicity Conclusion
 
PCOS, Lipid and Steroid metabolism 
 
Rotterdam Criteria 
Direct 
79 PCOs patients and 93 controls 
The results of qPCR showed that the expression of related genes were in accordance with the RNA-seq analysis results. 

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